potassium chloride

Generic: potassium chloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 600 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-056
Product ID 72789-056_40314483-9bfb-dbb4-e063-6394a90a827c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208864
Listing Expiration 2026-12-31
Marketing Start 2020-01-02

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789056
Hyphenated Format 72789-056

Supplemental Identifiers

RxCUI
315183
UNII
660YQ98I10

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA208864 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-01)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-30)
source: ndc

Packages (2)

72789-056-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-01) 72789-056-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-30)

Ingredients (1)

potassium chloride (600 mg/1)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40314483-9bfb-dbb4-e063-6394a90a827c", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["315183"], "spl_set_id": ["cc15ef60-6956-4d34-b86d-72cdd0c0c0bb"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-01)", "package_ndc": "72789-056-01", "marketing_start_date": "20200225"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-30)", "package_ndc": "72789-056-30", "marketing_start_date": "20230714"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "72789-056_40314483-9bfb-dbb4-e063-6394a90a827c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "72789-056", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA208864", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}